FDA 510(k)

EasyTeleMed (2.0.2)

Número K: K252440 · 2025-10-02

Data da decisão2025-10-02

Código do produtoDRG

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

EasyTeleMed (2.0.2) is the device name listed in this FDA 510(k) record. The listed applicant is Ingeniars S.R.L.. It received FDA 510(k) clearance on 2025-10-02 under 510(k) number K252440. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the EasyTeleMed (2.0.2)?

EasyTeleMed (2.0.2) is a medical device that received FDA 510(k) clearance on 2025-10-02. The listed applicant is Ingeniars S.R.L.. The 510(k) number is K252440.

When did EasyTeleMed (2.0.2) receive FDA 510(k) clearance?

EasyTeleMed (2.0.2) received FDA 510(k) clearance on 2025-10-02, under 510(k) number K252440.

Who is the listed applicant for EasyTeleMed (2.0.2)?

The FDA 510(k) record lists Ingeniars S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EasyTeleMed (2.0.2)?

The FDA product code for EasyTeleMed (2.0.2) is DRG.

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Fonte oficial

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